Canonical Allele Identifier: CA2082836050

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379431C= , CM000675.2:g.32379431C=	GRCh38
NC_000013.10:g.32953568C= , CM000675.1:g.32953568C=	GRCh37
NC_000013.9:g.31851568C=	NCBI36
NG_012772.3:g.68952C= , LRG_293:g.68952C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8869C=	ENSP00000434898.2:p.Gln2957=
ENST00000528762.2:c.*236C=	ENSP00000433168.2:n.*236C=
ENST00000530893.7:c.8500C=	ENSP00000499438.2:p.Gln2834=
ENST00000665585.2:c.*431C=	ENSP00000499570.2:n.*431C=
ENST00000666593.2:c.8869C=	ENSP00000499256.2:p.Gln2957=
ENST00000700202.2:c.8869C=	ENSP00000514856.2:p.Gln2957=
ENST00000700202.1:c.1336C=	ENSP00000514856.1:p.Gln446=
ENST00000700203.1:n.996C=
ENST00000380152.8:c.8869C= MANE Select	ENSP00000369497.3:p.Gln2957=
ENST00000544455.6:c.8869C=	ENSP00000439902.1:p.Gln2957=
ENST00000614259.2:c.8877C=	ENSP00000506251.1:n.8877C=
ENST00000665585.1:c.1747C=
ENST00000680887.1:c.8869C=	ENSP00000505508.1:p.Gln2957=
ENST00000380152.7:c.8869C=	ENSP00000369497.3:p.Gln2957=
ENST00000528762.1:c.431C=	ENSP00000433168.1:n.431C=
ENST00000544455.5:c.8869C=	ENSP00000439902.1:p.Gln2957=
NM_000059.3:c.8869C= , LRG_293t1:c.8869C=	NP_000050.2:p.Gln2957=
XM_011535203.1:c.8869C=	XP_011533505.1:p.Gln2957=
XM_011535204.1:c.8773C=	XP_011533506.1:p.Gln2925=
XM_011535205.1:c.8755-319C=	XP_011533507.1:n.8755-319C=
NM_000059.4:c.8869C= MANE Select	NP_000050.3:p.Gln2957=